简介:InordertosuppressthesurfacecrackinginducedbyCuduringreheatingandhotrollingprocess,Cuenrichmentanditsmigrationatthesteel-scaleinterfacewasinvestigatedduringheatingofsteelcastattemperaturesbetween1000℃and1200℃inN2-O2andN7-H2Oatmospheres.ForoxidationofCucontainingsteel,CuenrichedphasewasformedbythepreferentialoxidationofFeandtheenrichmentandmigrationbehaviorofCudependsontheoxidationtemperature,steelchemistryandatmospherecondition.NiinsteelinducedtheformationofsolidCuandNienrichedphaseatsteel/scaleinterfaceandinscalelayerandtheformationofunevensteel/scaleinterface,whichsuppressestheCuenrichmentbecauseofextrusionofCuenrichedregionbeforetheformationofliquidphase.Ontheotherhand,SnadditionpromotestheliquidCuformationatsteel/scaleinterfaceandpenetrationintograinboundaryofCuenrichedphasebydecreasingsolidustemperatureandsolubilitylimit.Inaddition,foroxidationat1200℃,thebehaviorofCuatandaroundthesteel-scaleinterfacewasfounddependenttoalargeextentonmorphologyoftheoxidescaleformedduringoxidation.Attheearlystageofoxidation,Cu-richphaseformedandaccumulatedatthesteelscaleinterfaceunderbothO2-N2andH2O-N2atmospheres.Astheoxidationproceeded,however,Cuenrichmentatanditsmigrationfromthesteel-scaleinterfacewerevastlydifferentfordifferentoxidizingatmospheres.InthecaseofO2-N2oxidation,anoxidelayerformedinitiallyatthesteelsurface,butsoonafteragapwasdevelopedatthesteel-scaleinterfaceandgrewinitssize,whichpracticallyseparatedthescalefromthesteelsubstrate.Thescalelayerformedunderthisconditionwasporous.TheCu-richphaseinitiallyformedattheinterfacewasfoundmigratingtothescalelayer,leavingnoCu-richphaseattheinterface.InthecaseofH2O-N2oxidation,however,thescalelayerformedwasdenseandtightlyattachedtothesteelsurface,andtheCurich-phasecontinuedto
简介:Aseriesofthecoconutactivatedcarbons(CAC)basedabsorbentsmodifiedwithCuandCe(Cu/CAC,Cu/Ce/CAC)werepreparedbyimpregnationtechnologyforcarbondioxidecapture.TheadsocrptionequilibriumsofCO2onCu/CACandCu/Ce/CACweremeasured.TheresultsshowedthattheadsorptioncapacityofCO2ontotheactivatedcarbonmodifiedwithCu/Ceincreasedwiththedecreasingtemperatureinthesamepressure.TheadsorptioncapacityofCO2onCu/CACwashigherthanthatoftheblankCAC,andcomparedwiththeCu/CAC,theadsorptioncapacityofCO2ofCu/Ce/CACwiththemassratioofCu/Ce=30wasimprovedat298and303K.Inaddition,theadsorptionequilibriumdataforCO2atvarioustemperatureswasfittedtoLangmuir,FreundlichandD-Risothermmodels.ItwasfoundthattheD-RequationwasthebestmodelforfittingtheadsorptiondataonCu/Ce/CACatdifferenttemperatures.
简介:对Cu-W-Ni-C与Ag-ZnO10触头材料的性能进行了对比和研究.在相对密度相同时,CuW-Ni-C材料的电阻率与Ag-ZnO10材料的电阻率接近,而硬度高于Ag-ZnO10材料的硬度.温升和通断能力试验结果表明:Cu-W-Ni-C材料在电力机车电器上完全可替代Ag-ZnO10材料.
简介:CuprecipitationbehaviorsintwoCu-bearingausteniticantibacterialstainlesssteels,type304andtype317L,weresystematicallystudiedbyusingrelativelysimplemethodsformaterialsanalysis,includingmicro-hardness,electricalresistivity,electrochemicalimpedancespectroscopy,X-raydiffractionanddifferentialscanningcalorimetry.Theresultsindicatedthatafteragingatelevatedtemperature,themicro-hardness,electricalresistivity,electrochemicalimpedanceandlatticeconstantofthesteelwereallvariedatdifferentdegreesduetotheprecipitationandgrowthofCu-richphases.TheresultsalsoshowedthattheheatevolutionduringtheprocessofCuprecipitationcouldbesensitivelydetectedbymeansofdifferentialscanningcalorimetry,obtainningthestartingtemperature,peaktemperature,peakareaoftheCu-richprecipitation,andeventheactivationenergybycalculation.TheresultsconfirmedthattheCu-richphasedprecipitationintheCu-bearingausteniticantibacterialstainlesssteelshouldbeathermalactivationprocesscontrolledbyCudiffusion.AllthematerialsanalysismethodsusedinthisstudycanbemoresimpleandeffectiveforapplicationinR&DoftheCu-bearingantibacterialstainlesssteels.
简介:Thereisanincreasingtrendforproducingcopper-containingsteels,withcopperbeingeitheraresidualelementfromscrapsoranintentionaladdition,i.e.,inweatheringsteel.Theissueofsurfacehotshortnessoccursduringthehotworkingofsteelscontainingcopper,andasignificantamountofworkhasbeenperformedonthistopic.Thispaperprovidesareviewofrelatedstudiesonthisphenomenon.Theformationmechanism,asanalyzed,istheliquidmetalembrittlementcausedbytheliquidcopperpenetrationintoaustenitegrainboundariesatthemetalsurface,wherethecopperoriginatesfromtheselectiveoxidationofthesteelathightemperature.Onthebasisofthemechanism,moreimportanceisplacedonanalyzingtheeffectonthephenomenonbyvaryingthecontrollingfactors,includingtheheatingprocess,alloyingadditions,anddeformationconditions.Possiblesolutionstotheproblemarefinalized,andsomefurtherworkmustbeperformedinthefuture.
简介:以金属铜箔和镍粉为原料,采用涂覆法制备出Ni—Cu多孔薄膜。采用场发射扫描电子显微镜(FE-SEM)、x射线衍射仪(XRD)、原予力显微镜(AFM)等设备对所制Ni-Cu薄膜的显微结构、物相组成进行表征。通过压泡法对所制多孔薄膜的通量及孔径进行测试,并探讨薄膜的成孔机理。研究表明:所制备Ni-Cu多孔薄膜厚度约为50μm,平均孔径约10girl;涂覆面通过Ni粉的松装烧结形成多孔结构;铜箔一测的孔是由于Kirkendall效应所产生的空位沿着晶界扩散在表面聚集而成。
简介:以FeMn合金粉末的形式在铁基合金粉末中添加Mn元素,退火后得到Fe-Cu-Mn部分预合金粉末,采用模壁润滑温压工艺制备Fe-Cu-Mn-C合金,通过对合金密度与硬度的测定以及形貌观察,研究Fe-Cu-Mn-C粉末的压制与烧结行为,以及Mn含量对合金密度和力学性能的影响。结果表明,通过退火处理实现部分预合金扩散而得到的Fe-Cu-Mn粉末具有很好的压制性能,Fe-2Cu-0.5Mn-0.9C压坯密度达到7.37g/cm3,烧结密度为7.33g/cm3;添加适量Mn能有效提升铁基合金的力学性能,其中Fe-2Cu-0.5Mn-0.9C合金的性能最佳,抗拉强度达到715MPa;随Mn含量增加,合金的孔隙增多、密度下降,导致强度和硬度下降。合金的局部氧化对性能产生一定的负面影响。Mn含量对合金组织影响不大,Fe-2Cu-Mn-0.9C合金呈现混合显微组织,由铁素体、珠光体和少量贝氏体构成。Mn的蒸发与凝聚是Fe-Cu-Mn-C的烧结机制。
简介:VariousopticalluminescencespectroscopictechniqueswereusedtocharacterizethehighTcsuperconductorYBa2Cu3Ox.TheemissionbandsrevealthatCu3+coexistwithCu2+andCu+inthismaterial.
简介:在元素粉末反应制备多孔材料中,原料粉末粒度是影响其多孔结构的主要因素之一。本文通过元素粉末反应合成的方法制备Cu-Al多孔材料,研究原料粉末的粒径对Cu-Al多孔材料孔径、孔隙度、透气度和体积膨胀率等参数的影响。结果表明:Al粉粒径是影响Cu-Al多孔材料最大孔径的主要因素,材料的最大孔径dm与Al粉粒径dp之间严格遵循dm=0.48dp的线性变化规律;Cu粉粒径则对Cu-Al多孔材料最大孔径影响较小。当粉末粒径在48.5μm以上时,粉末粒径的改变对Cu-Al多孔材料的开孔隙度和总孔隙度影响不大。在实验研究范围内,Cu-Al多孔材料的体积膨胀率随粉末粒径的增大而增大;当粉末粒径很小时,Cu-Al多孔材料存在体积收缩的趋势。
简介:采用等离子喷涂技术,在C/C-Cu复合材料表面制备W涂层,采用氧乙炔焰进行烧蚀考核,通过金相显微镜、扫描电镜及X射线衍射仪对烧蚀前后涂层的显微组织及相组成进行分析,并与没有W涂层的C/C-Cu复合材料进行对比。结果表明,熔蚀后有涂层的C/C-Cu复合材料质量损失仅0.9mg/s,无涂层C/C-Cu试样的质量损失为5.6mg/s。C/C-Cu复合材料表面W涂层较致密,与基体结合良好。烧蚀后C/C-Cu表面W涂层主要生成WO3和CuWO4,能谱分析(EDAX)表明有较多的Cu元素存在,但分布不均匀。W涂层在烧蚀后均较粗糙、疏松,存在孔洞和裂纹等缺陷,成为降低性能的重要因素。
简介:利用粉末冶金方法研制了Sm(CobalFe0.24Cu0.08Zr0.027)7.0,Sm(CpbalFe0.27Cu0.05Zr0.027)7.0,Sm(CobalFe0.26Cu0.05Zr0.026)7.03种高温永磁,并对其磁性能、温度稳定性和显微结构进行了分析.结果表明:样品Sm(CobalFe0.27Cu0.05Zr0.027)7.0具有最高的内禀矫顽力(2165.6kA·m-1)和最大磁能积(212.0kA·m-3);3种磁体的温度系数都较低,最高使用温度均在400℃以上,大大高于一般商用磁体;增加Sm,Co,Cu的含量和减少Fe的含量可以提高材料的温度稳定性.X射线分析表明,合金中含有Sm2(Co,Fe)17主相,Sm(Co,Cu)5相,含Zr化合物等.Sm(Co,Cu)5相、单质Zr、晶粒边界等钉扎畴壁,使合金具有较高的矫顽力.
简介:Fe/Cu/Cemodifiedcoal-basedactivatedcarbon(AC)waspreparedbythesol-gelmethod,andtheeffectofFe/Cu/CeoncatalyticpropertiesofFe/AC,Fe-Cu/ACandFe-Cu-Ce/ACwasinvestigatedinthehydrolysisofcarbonylsulfide(COS)at50°C.Theirsurfacepropertieswereevaluatedbymeansofnitrogenadsorptionandwerecharacterizedbyusingscanningelectronmicroscopy(SEM),X-raydiffracto-metry(XRD)andX-rayphotoelectronspectroscopy(XPS).ThecatalyticactivitiesresultsshowedthatadditionofCuandCe...
简介:以七钼酸铵和硝酸铜为原料通过溶胶-凝胶法制备Cu含量(质量分数)为20%的超细Mo-Cu复合粉末,再在1050-1200℃下烧结粉末压坯制得Mo-Cu复合材料;通过热重分析(DTA-TG)、X-ray衍射分析(XRD)和透射电镜(TEM)等分别对干凝胶煅烧前后的粉体以及还原后所得Mo-Cu复合粉末进行表征,通过扫描电镜观察Mo-Cu烧结体的显微组织,并对其密度、物理和力学性能进行测定,探索制备高致密、高性能Mo-Cu复合材料新工艺。结果表明:通过溶胶-凝胶法可以制得平均粒度为150nm、组成均匀的Mo-Cu超细粉末,该粉末具有良好的烧结性能,其成形压坯在1200℃下于H2气氛中烧结90min后,相对密度可达99.78%,烧结体的抗弯强度和维氏硬度分别为988MPa和HV227,电导率和导热系数分别为42.56%IACS和157W/(m·K),室温至450℃的热膨胀系数在6.7×10^-6-7.6×10^-6K^-1之间。